Craniosynostosis requires evaluation by specialists, such as a pediatric neurosurgeon or plastic surgeon. Diagnosis of craniosynostosis may include:
- Physical exam. Your doctor will feel your baby's head for abnormalities such as suture ridges, and look for facial deformities.
- Imaging studies. A computerized tomography (CT) scan of your baby's skull can show whether any sutures have fused. Fused sutures are identifiable by their absence, because they're invisible once fused, or by the ridging of the suture line. A laser scan and photographs also may be used to make precise measurements of the skull shape.
- Genetic testing. If your doctor suspects an underlying genetic syndrome, genetic testing may help identify the syndrome.
Mild cases of craniosynostosis may not need treatment. Your doctor may recommend a specially molded helmet to help reshape your baby's head if the cranial sutures are open and the head shape is abnormal. In this situation, the molded helmet can assist your baby's brain growth and correct the shape of the skull.
However, for most babies, surgery is the primary treatment. The type and timing of surgery depends on the type of craniosynostosis and whether there's an underlying genetic syndrome.
The purpose of surgery is to correct the abnormal head shape, reduce or prevent pressure on the brain, create room for the brain to grow normally and improve your baby's appearance. This involves a process of planning and surgery.
Imaging studies can help surgeons develop a surgical procedure plan. Virtual surgical planning for treatment of craniosynostosis uses high-definition 3-D CT scans of your baby's skull to construct a computer-simulated, individualized surgical plan. Based on that virtual surgical plan, customized templates are constructed to guide the procedure.
A team that includes a specialist in surgery of the head and face (craniofacial surgeon) and a specialist in brain surgery (neurosurgeon) generally performs the procedure. Surgery can be done by endoscopic or open surgery. Both types of procedures generally produce very good cosmetic results with low risk of complications.
- Endoscopic surgery. This minimally invasive surgery may be considered for babies up to age 6 months who have single-suture craniosynostosis. Using a lighted tube and camera (endoscope) inserted through small scalp incisions, the surgeon opens the affected suture to enable your baby's brain to grow normally. Compared with an open procedure, endoscopic surgery has a smaller incision, typically involves only a one-night hospital stay and usually does not require a blood transfusion.
- Open surgery. Generally, for babies older than 6 months, open surgery is done. The surgeon makes an incision in the scalp and cranial bones, then reshapes the affected portion of the skull. The skull position is held in place with plates and screws that are absorbable. Open surgery typically involves a three- or four-day hospital stay, and blood transfusion is usually necessary. It's generally a one-time procedure, but in complex cases, multiple open surgeries are often required to correct the baby's head shape.
After endoscopic surgery, visits at certain intervals are required to fit a series of helmets to help shape your baby's skull. If open surgery is done, no helmet is needed afterward.
Coping and support
When you learn that your baby has craniosynostosis, you may experience a range of emotions, including anger, fear, worry, sorrow and guilt. You may not know what to expect, and you may worry about your ability to care for your baby. The best antidote for fear and worry is information and support.
Consider these steps to prepare yourself and to care for your baby:
- Find a team of trusted professionals. You'll need to make important decisions about your baby's care. Medical centers with craniofacial specialty teams can offer you information about the disorder, coordinate your baby's care among specialists, help you evaluate options and provide treatment.
- Seek out other families. Talking to people who are dealing with similar challenges can provide you with information and emotional support. Ask your doctor about support groups in your community. If a group isn't for you, maybe your doctor can put you in touch with a family who has dealt with craniosynostosis. Or you may be able to find group or individual support online.
- Expect a bright future. Most children have normal cognitive development and achieve good cosmetic results after surgery. Early diagnosis and treatment are key.
Preparing for your appointment
In some cases, your baby's pediatrician may suspect craniosynostosis at a routine well-baby visit. In other cases, you may make an appointment because you have concerns about your baby's head growth. Your doctor can refer you to a specialist for diagnosis and treatment.
Here's some information to help you get ready for your appointment. If possible, bring a family member or friend with you. A trusted companion can help you remember information and provide emotional support.
What you can do
Before the appointment, make a list of:
- Any signs you've noticed, such as raised ridges or the absence of soft spots on your baby's head
- Questions to ask your doctor
Questions to ask might include:
- What's the most likely cause of my baby's symptoms?
- Are there other possible causes?
- What kinds of tests does my baby need? Do these tests require any special preparation?
- Is this condition temporary or long lasting?
- What treatments are available, and which do you recommend?
- Are there alternatives to the treatment you're recommending?
- What are the risks involved with surgery?
- Who will perform the surgery if it's needed?
- What happens if we choose not to have the surgery right now?
- Will the abnormal shape of the skull affect the functioning of my baby's brain?
- What is the likelihood of future children having the same condition?
- Are there brochures or other printed material that I can have?
- What websites do you recommend?
Don't hesitate to ask other questions during the appointment.
What to expect from your doctor
Your doctor is likely to ask you questions, as well. Be ready to answer them to reserve time to go over points you want to spend more time on. Your doctor may ask:
- When did you first notice the changes in your baby's head?
- How much time does your baby spend on his or her back?
- In what position does your baby sleep?
- Has your baby had any seizures?
- Is your baby's development on schedule?
- Were there any complications during your pregnancy?
- Do you have a family history of craniosynostosis or genetic conditions such as Apert syndrome, Pfeiffer syndrome or Crouzon syndrome?